Specialized Analytical Testing for Complex, High‑Value Projects
Accurate, defensible results powered by advanced mass spectrometry, chromatography, and fit‑for‑purpose analytical methods
SECTION 1 — About Us / Value Proposition
Precise Science. Trusted Results. Faster Decisions.
Analytical RnD delivers specialized analytical testing solutions across clinical, biopharma, pharmaceutical, medical device, and food sectors.
We design, validate, and execute fit‑for‑purpose analytical methods that accelerate R&D, reduce regulatory risk, and ensure product quality from early concept through commercialization.
CTA:
[Explore Our Capabilities]
SECTION 2 — Core Services
Comprehensive Analytical Services
Analytical Method Development
- New analytes & challenging matrices
- Extraction, cleanup, and sample‑prep innovation
Method Validation & Verification
- Full validation packages (accuracy, precision, specificity, linearity, range)
- LOD/LOQ and robustness assessments
Sample Analysis & Contract Testing
- Batch/lot release
- Stability timepoints
- Comparability & bridging studies
Characterization & Investigations
- Unknown ID & degradant elucidation
- Impurity profiling and root‑cause analyses
Regulatory Support
- Protocols, validation summaries
- Submission‑ready data packages
CTA:
[See Detailed Service Offerings]
SECTION 3 — Instrumentation & Technologies
Advanced Technology for High‑Confidence Results
- High‑Resolution Mass Spectrometry (Orbitrap)
Accurate-mass, structural insights, metabolite ID - Triple Quadrupole MS/MS
High‑throughput targeted quantitation (MRM) - Chromatography Platforms
LC (HPLC/UPLC), GC/HS‑GC, Ion Chromatography - Sample Prep & Automation
Automated liquid handling, SPE, ultrasonication - Data Integrity & Compliance
21 CFR Part 11‑aligned systems, audit trails, controlled templates
CTA:
[View Our Instrument Suite]
SECTION 4 — Sector Applications
Industry Expertise Across Regulated & Complex Markets
Clinical & Biopharma
Impurity profiling, metabolite ID, E&L studies
Pharmaceuticals
API/DP assay & impurities, cleaning validation, dissolution support
Medical Devices
Materials characterization, sterilization by‑products, E&L
Food & Nutrition
Contaminants, residues, additives, shelf‑life & degradation pathways
CTA:
[See Case Studies]
SECTION 5 — Quality & Compliance
Quality You Can Trust
Our quality framework aligns to ISO/IEC 17025 principles, ensuring defensible, traceable, and reproducible data.
- Risk‑assessed workflows & chain‑of‑custody tracking
- Validated waste handling & controlled documentation
- Strict confidentiality & secure data environments
- Licensed by APVMA to manufacture veterinary chemical products
(Licence No: [Insert Number])
CTA:
[Learn About Our Quality System]
SECTION 6 — Why Clients Choose Us
Our Differentiators
- Deep expertise in HRMS & MS/MS workflows
- Strong capability with complex matrices (biologicals, polymers, high‑fat foods)
- Faster cycle times through parallel development/validation
- Decision‑ready reporting with spectral and statistical justification
- Flexible engagement models: feasibility → validation → routine testing
CTA:
[Partner With Us]
SECTION 7 — Contact / Lead Form
Ready to Start Your Project?
Our scientists are ready to help you design the right analytical strategy.
Primary CTA:
[Request a Consultation]
Secondary CTA:
[Send Us Your Enquiry]
Analytical Equipment
Molecular Biology
and Invitro studies
General Equipment
Why should You choose us?
- NATA accredited lab under ISO/IEC 17025
- We have experts and advanced technology which will meet your expectations on your next beverages testing.
- We do all required research and analysis to ensure the methdologies fit for purpourse for each project.
- We can match high standard quality compliance and help you with new product development.
- We can provide you with quick results on the required tests before exporting your products.
